Chemical Formula: C25H28O4
Chemical Formula C25H28O4
Found 130 metabolite its formula value is C25H28O4
(R)-Hispaglabridin A
(R)-Hispaglabridin A is found in herbs and spices. (R)-Hispaglabridin A is isolated from Glycyrrhiza glabra (licorice). Isolated from Glycyrrhiza glabra (licorice). (R)-Hispaglabridin A is found in tea and herbs and spices.
Chakasaponin VI
Chakasaponin vi is a member of the class of compounds known as 2-hydroxychalcones. 2-hydroxychalcones are organic compounds containing chalcone skeleton that carries a hydroxyl group at the 2-position. Thus, chakasaponin vi is considered to be a flavonoid lipid molecule. Chakasaponin vi is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). Chakasaponin vi can be found in tea, which makes chakasaponin vi a potential biomarker for the consumption of this food product.
Mulberrofuran A
Mulberrofuran A is found in fruits. Mulberrofuran A is a constituent of white mulberry (Morus alba). Constituent of white mulberry (Morus alba). Mulberrofuran A is found in mulberry and fruits.
Erythrabyssin II
Erythrabyssin II is a member of pterocarpans. Erythrabyssin II is a natural product found in Erythrina abyssinica, Erythrina suberosa, and other organisms with data available. Erythrabyssin II is found in pulses. Erythrabyssin II is isolated from Phaseolus lunatus (butter bean). Isolated from Phaseolus lunatus (butter bean). Erythrabyssin II is found in pulses.
(S)-4',7-Dihydroxy-3',8-diprenylflavanone
(S)-4,7-Dihydroxy-3,8-diprenylflavanone is found in herbs and spices. (S)-4,7-Dihydroxy-3,8-diprenylflavanone is a constituent of roots of Glycyrrhiza glabra (licorice) Glabrol (Compound 1), One isoprenyl flavonoid was isolated from ethanol extract of licorice roots, is a potent and non-competitive Acyl-coenzyme A: cholesterol acyltransferase (ACAT) inhibitor with an IC50 value of 24.6 μM for rat liver microsomal ACAT activity[1]. Glabrol (Compound 1), One isoprenyl flavonoid was isolated from ethanol extract of licorice roots, is a potent and non-competitive Acyl-coenzyme A: cholesterol acyltransferase (ACAT) inhibitor with an IC50 value of 24.6 μM for rat liver microsomal ACAT activity[1]. Glabrol (Compound 1), One isoprenyl flavonoid was isolated from ethanol extract of licorice roots, is a potent and non-competitive Acyl-coenzyme A: cholesterol acyltransferase (ACAT) inhibitor with an IC50 value of 24.6 μM for rat liver microsomal ACAT activity[1].
(2E)-1-[3-(3,7-dimethylocta-2,6-dien-1-yl)-2,4,6-trihydroxyphenyl]-3-phenylprop-2-en-1-one
Erybraedin A
Erybraedin A is found in lima bean. Erybraedin A is isolated from Phaseolus lunatus (butter bean). Isolated from Phaseolus lunatus (butter bean). Erybraedin A is found in pulses and lima bean.
(S)-8-Prenylphaseollinisoflavan
(S)-8-Prenylphaseollinisoflavan is found in herbs and spices. (S)-8-Prenylphaseollinisoflavan is a constituent of Glycyrrhiza glabra (licorice). Constituent of Glycyrrhiza glabra (licorice). (S)-8-Prenylphaseollinisoflavan is found in tea and herbs and spices.
CC(C)=CCCC(C)=CCc1c(O)ccc(C(=O)C=Cc2ccc(O)cc2)c1O
[(8S,9S,13S,14S,17R)-3,17-Dihydroxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-1-yl] benzoate
4-(gamma,gamma-Dimethylallyl)-phaseollidin
4-(gamma,gamma-dimethylallyl)-phaseollidin, also known as 4-prenylphaseollidin, is a member of the class of compounds known as pterocarpans. Pterocarpans are benzo-pyrano-furano-benzene compounds, containing the 6H-[1]benzofuro[3,2-c]chromene skeleton. They are derivatives of isoflavonoids. 4-(gamma,gamma-dimethylallyl)-phaseollidin is practically insoluble (in water) and a very weakly acidic compound (based on its pKa). 4-(gamma,gamma-dimethylallyl)-phaseollidin can be found in lima bean, which makes 4-(gamma,gamma-dimethylallyl)-phaseollidin a potential biomarker for the consumption of this food product.
Glabrol
Glabrol is a member of flavanones. Glabrol is a natural product found in Sophora alopecuroides, Euchresta formosana, and other organisms with data available. See also: Glycyrrhiza Glabra (part of). Glabrol (Compound 1), One isoprenyl flavonoid was isolated from ethanol extract of licorice roots, is a potent and non-competitive Acyl-coenzyme A: cholesterol acyltransferase (ACAT) inhibitor with an IC50 value of 24.6 μM for rat liver microsomal ACAT activity[1]. Glabrol (Compound 1), One isoprenyl flavonoid was isolated from ethanol extract of licorice roots, is a potent and non-competitive Acyl-coenzyme A: cholesterol acyltransferase (ACAT) inhibitor with an IC50 value of 24.6 μM for rat liver microsomal ACAT activity[1]. Glabrol (Compound 1), One isoprenyl flavonoid was isolated from ethanol extract of licorice roots, is a potent and non-competitive Acyl-coenzyme A: cholesterol acyltransferase (ACAT) inhibitor with an IC50 value of 24.6 μM for rat liver microsomal ACAT activity[1].
Kanzonol
Kanzonol C is a natural product found in Brosimum gaudichaudii, Fatoua pilosa, and other organisms with data available.
7-Prenyloxy-8-C-(3-hydroxy-3-methyl-trans-buten-1-yl)flavanone
linderatone
2(S)-6-Carboxy-7-hydroxy-2-methyl-2-(4-methyl-3-pentenyl)-5-(2-phenylethyl)chromene
Xanthoangelol
Xanthoangelol, extracted from Angelica keiskei, suppresses obesity-induced inflammatory responses. Xanthoangelol possesses antibacterial activity[1][2]. Xanthoangelol inhibits monoamine oxidases[3]. Xanthoangelol induces apoptosis in neuroblastoma and leukemia cells[4].
Kanzonol C
Kanzonol C is a natural product found in Brosimum gaudichaudii, Fatoua pilosa, and other organisms with data available.
Bis(6,6-dimethyl-4,5-dihydropyrano)[2,3:4,5][2,3:4,3]-2-hydroxychalcone
Isocycloglabrol
Flemiwallichin E
Linderachalcone
Abyssinone VI
A member of the class of chalcones that is isolated from the stem of Erythrina abyssinica.
Erybraedin A
A member of the class of pterocarpans that is 3,9-dihydroxypterocarpan substituted with prenyl groups at positions 4 and 10 (the 6aR,11aR stereoisomer). Isolated from Erythrina stricta and Erythrina zeyheri, it exhibits antibacterial, antimycobacterial, antiplasmodial and cytotoxic activities.
Hispaglabridin A
(S)-form-Prostratol F|8-geranyl-4,7-dihydroxyflavanone|8-[(2E)-3,7-Dimethylocta-2,6-dien-1-yl]-2,3-dihydro-7-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one|prostratol F
2-(3,7-Dimethyl-2,6-octadienyl)-1,3,8-trihydroxy-6-methyl-9(10H)-anthracenone|2-geranylemodin anthrone
(3R)-2,7-dihydroxy-3-(methylbut-2-enyl)-2,2-dimethylpyrano[5,6:4,5]isoflavan
1-[2,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl]-3-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]prop-2-en-1-one
(E)-1-(5-((E)-3,7-dimethylocta-2,6-dien-1-yl)-2,4-dihydroxyphenyl)-3-(4 hydroxyphenyl)prop-2-en-1-one|2?,4?,4-trihydroxy-5?-geranylchalcone|5-geranyl-2,4,4-trihydroxychalcone|isoxanthoangelol
Kazinol B
Kazinol B is a natural product found in Broussonetia papyrifera and Broussonetia kazinoki with data available.
4-Geranyloxyisoliquiritigenin|4-O-Geranylisoliquiritigenin|4-O-geranylisoquiritigenin
7-O-(3-methyl-2-butenyl)-(S,E)-7-Hydroxy-8-(3-hydroxy-3-methyl-1-butenyl)flavanone
Xanthoangelol
Xanthoangelol is a natural product found in Artocarpus altilis, Artocarpus nobilis, and other organisms with data available. See also: Angelica keiskei top (part of); Angelica keiskei root (part of). D004791 - Enzyme Inhibitors > D054328 - Proton Pump Inhibitors Xanthoangelol, extracted from Angelica keiskei, suppresses obesity-induced inflammatory responses. Xanthoangelol possesses antibacterial activity[1][2]. Xanthoangelol inhibits monoamine oxidases[3]. Xanthoangelol induces apoptosis in neuroblastoma and leukemia cells[4].
Hispaglabridin A
Hispaglabridin A is a member of the class of hydroxyisoflavans that is (R)-isoflavan substituted by hydroxy groups at positions 2 and 4 , a 3-methylbut-2-en-1-yl group at position 3 and a 2,2-dimethyl-2H-pyran group across positions 7 and 8 respectively. It has a role as a plant metabolite. It derives from a hydride of a (R)-isoflavan. Hispaglabridin A is a natural product found in Glycyrrhiza glabra with data available. See also: Glycyrrhiza Glabra (part of). A member of the class of hydroxyisoflavans that is (R)-isoflavan substituted by hydroxy groups at positions 2 and 4 , a 3-methylbut-2-en-1-yl group at position 3 and a 2,2-dimethyl-2H-pyran group across positions 7 and 8 respectively.
8-[(2E)-3,7-dimethylocta-2,6-dienyl]-5,7-dihydroxy-2-phenyl-2,3-dihydrochromen-4-one
3-[(2E)-3,7-dimethylocta-2,6-dienyl]-2,4-dihydroxy-6-[(E)-2-phenylethenyl]benzoic acid
2,4-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol
2,4-bis(3-methylbut-2-enyl)-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol
(S)-8-Prenylphaseollinisoflavan
Mulberrofuran A
AIDS-096018
[(8S,9S,13S,14S,17R)-3,17-Dihydroxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-1-yl] benzoate
(2S)-5,7-Dihydroxy-8-[(2E)-3,7-dimethyl-2,6-octadienyl]flavanone
3-(3,7-Dimethyl-2,6-octadienyl)-2,4-dihydroxy-6-(2
(2S)-7,4-Dihydroxy-8-geranylflavanone
A dihydroxyflavanone that is (2S)-flavanone substituted by hydroxy groups at position 7 and 4 and a geranyl group at position 8.